Chinese Migrant Population Health Cohort
2 other identifiers
observational
26,000
1 country
1
Brief Summary
The Chinese Migrant Population Health Cohort is a prospective, multi-center study jointly initiated by Professor Yong Ji, President of Harbin Medical University, and Academician Guoqiang Chen, President of Hainan Medical University, in collaboration with regional partners. It targets older adults (≥60 years) who engage in seasonal migration between cold (Heilongjiang) and tropical (Hainan) regions. The primary objective is to investigate cardiovascular and metabolic disease risks, underlying biological and environmental mechanisms, and effective preventive strategies in this unique population. Participants are recruited from both origin and destination sites and undergo standardized baseline assessments, including questionnaires, physical examinations, medical imaging, biospecimen collection (blood, stool, hair, nails), and environmental exposure monitoring. Longitudinal follow-up includes periodic reassessments, remote monitoring, and data linkage with hospital information systems to capture health outcomes. The study aims to: Define migration-related health risk profiles and disease phenotypes. Elucidate biological and environmental mechanisms influencing disease onset and progression. Develop AI-driven risk prediction models and evaluate targeted interventions through nested randomized controlled trials. Translate findings into clinical guidelines and scalable cross-regional health management models. This is the first cohort in China to systematically investigate the health impacts of seasonal migration in older adults. By integrating epidemiology, multi-omics, environmental data, and health policy translation, the study seeks to improve continuity of care, strengthen climate adaptation, and promote healthy ageing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 23, 2025
CompletedFirst Submitted
Initial submission to the registry
August 11, 2025
CompletedFirst Posted
Study publicly available on registry
August 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 30, 2030
August 20, 2025
August 1, 2025
4.8 years
August 11, 2025
August 14, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of Participants Experiencing First Major Cardiovascular Event
First occurrence of myocardial infarction, stroke (ischemic or hemorrhagic), or cardiovascular death, confirmed through hospital records, death registries, and adjudication committee review.
Up to 5 years from baseline
Secondary Outcomes (5)
Number of Participants with New-Onset Metabolic Disorders
Up to 5 years from baseline
Number of Deaths from Any Cause
Up to 5 years from baseline
Changes in Cardiometabolic Risk Factors
Baseline, 2 years, 4 years
Change in EQ-5D Quality of Life Score from Baseline
Baseline, 2 years, 4 years
Change in Cognitive Function Score (MoCA) from Baseline
Baseline, 2 years, 4 years
Other Outcomes (3)
Change in Carotid Intima-Media Thickness from Baseline
Baseline and follow-up imaging
Change in Coronary Artery Calcium Score from Baseline
Baseline and follow-up imaging
Change in Plasma Metabolite Levels from Baseline
Baseline and follow-up biospecimen analyses
Study Arms (4)
Winter Migrant Group
No Intervention
Summer Migrant Group
No Intervention
Cold-Region Resident Group
no Intervention
Tropical-Region Resident Group
no Intervention
Interventions
no intervention
Eligibility Criteria
The study will enroll community-dwelling adults aged ≥60 years from Harbin (cold region) and Hainan (tropical region), China. Four groups will be included: 1. Winter Migrant Group: \~5,000 Harbin residents who habitually migrate to Hainan during the cold season for ≥2 months each time, with ≥2 consecutive years of such migration and plans to continue; 2. Summer Migrant Group: \~1,000 Hainan residents who habitually migrate to Harbin during the hot season for ≥2 months, with similar migration history and plans; 3. Cold-Region Resident Group: \~10,000 Harbin residents, including matched controls for migrant groups and randomly selected residents, with no \>2 months residence outside Harbin in the past 5 years; 4. Tropical-Region Resident Group: \~10,000 Hainan residents with similar matching criteria and residency requirements. All participants must be able to communicate, perform daily activities independently, consent to long-term follow-up, and provide biospecimens.
You may qualify if:
- Permanent residents of Harbin or Hainan who will continue to reside in Harbin or Hainan for the next 5 years.
- Baseline age ≥60 years, with basic communication and comprehension abilities.
- No confirmed diagnosis of end-stage major organic diseases (e.g., advanced heart failure, advanced liver failure, advanced kidney failure, malignant tumors).
- Able to perform activities of daily living independently and capable of completing questionnaires and physical examinations.
- Willing to participate in the study, provide written informed consent, accept long-term follow-up, and provide biological specimens.
You may not qualify if:
- Occurrence of life-threatening acute events (e.g., myocardial infarction, acute heart failure, stroke) within the past 30 days.
- Currently receiving chronic treatment with antiviral drugs (e.g., for HIV) or antipsychotic medications.
- Presence of moderate to severe cognitive impairment preventing survey completion or follow-up cooperation.
- Current acute infectious diseases such as influenza or fever.
- Simultaneous participation in other interventional clinical studies.
- Refusal to sign informed consent or unwillingness to provide biological specimens.
- Any other condition deemed unsuitable for study participation by the investigators based on overall assessment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Jinwei Tianlead
- Hainan Medical Collegecollaborator
Study Sites (1)
Harbin Medical University
Harbin, Heilongjiang, 150086,, China
Related Publications (21)
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Biospecimen
Whole blood (serum, plasma, buffy coat, and peripheral blood mononuclear cells), urine, stool, hair, and nail samples will be collected and stored. Blood samples will be processed for biochemical assays, DNA, RNA, and multi-omics analyses (including metabolomics, proteomics, and lipidomics). Urine and stool samples will be analyzed for metabolic, microbiome, and environmental exposure markers. Hair and nail samples will be used for long-term exposure assessment (e.g., heavy metals, stable isotopes). All biospecimens will be stored in a certified biobank at -80 °C for future research.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Doctor
Study Record Dates
First Submitted
August 11, 2025
First Posted
August 15, 2025
Study Start
July 23, 2025
Primary Completion (Estimated)
April 30, 2030
Study Completion (Estimated)
April 30, 2030
Last Updated
August 20, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share